Lens assembly for biological testing
    1.
    发明专利
    Lens assembly for biological testing 审中-公开
    镜头组件进行生物测试

    公开(公告)号:JP2009216711A

    公开(公告)日:2009-09-24

    申请号:JP2009115052

    申请日:2009-05-11

    Inventor: SANDELL DONALD

    Abstract: PROBLEM TO BE SOLVED: To solve complexity of a lens in an optical detection system for a thermal cycling device. SOLUTION: The optical detection system for the thermal cycling device includes at least one light source 16, a light detection device 12 for detecting light received from a plurality of biological samples, and a lens 20 having a first surface 22 and a second surface 24 formed thereon, the second surface being practically opposed to the first surface. The first surface collimates the light and the second surface leads the light to each of the plurality of biological samples 60. COPYRIGHT: (C)2009,JPO&INPIT

    Abstract translation: 要解决的问题:为了解决用于热循环装置的光学检测系统中的透镜的复杂性。 解决方案:用于热循环装置的光学检测系统包括至少一个光源16,用于检测从多个生物样品接收的光的光检测装置12和具有第一表面22和第二表面22的透镜20 形成在其上的表面24,第二表面实际上与第一表面相对。 第一表面准直光,第二表面将光引导到多个生物样品60中的每一个上。版权所有:(C)2009,JPO&INPIT

    Substituted propargyletheoxyamido nucleoside
    2.
    发明专利
    Substituted propargyletheoxyamido nucleoside 有权
    取代的丙氧基甲酰胺核苷

    公开(公告)号:JP2009143946A

    公开(公告)日:2009-07-02

    申请号:JP2009026772

    申请日:2009-02-06

    CPC classification number: C07H21/00 C07H19/04 C12Q1/6869 Y02P20/55

    Abstract: PROBLEM TO BE SOLVED: To provide a labeled polynucleotide. SOLUTION: A substituted propargylethoxyamido nucleoside with a structure represented by figure (I) is disclosed, in which X is selected from the group consisting of an aminoalkanoic acid, an alkylaminobenzoic acid, α-benzoic acid, and 4-amino-2-butynic acid; R 1 and R 2 are each individually selected from the group consisting of -H, a lower alkyl group, a protective group, and a label; R 3 is selected from the group consisting of -H and a lower alkyl group; and B is 7-deazapurine, purine, or a pyrimidine nucleoside base. In addition, a primer extension method is provided, which uses the above X-substituted propargylethoxyamido nucleoside, and a polynucleotide containing the above X-substituted propargylethoxyamido nucleoside is provided. COPYRIGHT: (C)2009,JPO&INPIT

    Abstract translation: 待解决的问题:提供标记的多核苷酸。 解决方案:公开了具有由图(I)表示的结构的取代的炔丙氧基酰胺基核苷,其中X选自氨基链烷酸,烷基氨基苯甲酸,α-苯甲酸和4-氨基-2 - 丁酸; R 1 和R SB 2各自分别选自-H,低级烷基,保护基和标记; R SB 3选自-H和低级烷基; B是7-脱氮嘌呤,嘌呤或嘧啶核苷碱基。 此外,提供了使用上述X取代的炔丙氧基酰氨基核苷的引物延伸方法,并且提供了含有上述X取代的炔丙氧基酰氨基核苷的多核苷酸。 版权所有(C)2009,JPO&INPIT

    Digital assay
    3.
    发明专利
    Digital assay 审中-公开
    数字测定

    公开(公告)号:JP2009229468A

    公开(公告)日:2009-10-08

    申请号:JP2009124765

    申请日:2009-05-22

    Abstract: PROBLEM TO BE SOLVED: To provide a method and a composition for detecting a target in a sample. SOLUTION: A method for quantifying the target comprises forming a reaction mixture comprising a sample possibly containing the target, a codable label, one or more target-specific probes each of which binds specifically to the target under selective binding conditions, and a separating portion; treating the reaction mixture under reaction conditions such that a detectable complex is produced when the target is present, wherein the detectable complex includes the codable label, the target-specific probe and the separating portion; and counting the number of codable labels to quantify the target. COPYRIGHT: (C)2010,JPO&INPIT

    Abstract translation: 要解决的问题:提供用于检测样品中的靶的方法和组合物。 解决方案:用于定量靶的方法包括形成包含可能含有靶的样品,可编码标记,一种或多种在选择性结合条件下特异性结合靶的靶特异性探针的反应混合物,以及 分离部分 在反应条件下处理反应混合物,使得当靶存在时产生可检测的复合物,其中可检测的复合物包括可编码标记,靶特异性探针和分离部分; 并计算可编码标签的数量以量化目标。 版权所有(C)2010,JPO&INPIT

    短串聯重複基因座多工放大方法及套組 METHOD AND KITS FOR MULTIPLEX AMPLIFICATION OF SHORT TANDEM REPEAT LOCI
    5.
    发明专利
    短串聯重複基因座多工放大方法及套組 METHOD AND KITS FOR MULTIPLEX AMPLIFICATION OF SHORT TANDEM REPEAT LOCI 审中-公开
    短串联重复基因座多任务放大方法及套组 METHOD AND KITS FOR MULTIPLEX AMPLIFICATION OF SHORT TANDEM REPEAT LOCI

    公开(公告)号:TW200930818A

    公开(公告)日:2009-07-16

    申请号:TW097141704

    申请日:2008-10-29

    IPC: C12Q G01N

    CPC classification number: C12Q1/6876 C12Q2600/156

    Abstract: 揭示一些方法及材料以用於在單一多工反應同時放大基因體DNA的至少11種特定STR基因座,做為用於分析此種反應產物的材料及方法。包含於本發明的是在單一多工反應同時放大16種特定基因座的方法及材料,其包含10 AmpFlSTR^ SGMplus^ STR基因座、Amelogenin基因座、及5種新的STR基因座,其包含用於分析這些基因座的方法及材料。

    Abstract in simplified Chinese: 揭示一些方法及材料以用于在单一多任务反应同时放大基因体DNA的至少11种特定STR基因座,做为用于分析此种反应产物的材料及方法。包含于本发明的是在单一多任务反应同时放大16种特定基因座的方法及材料,其包含10 AmpFlSTR^ SGMplus^ STR基因座、Amelogenin基因座、及5种新的STR基因座,其包含用于分析这些基因座的方法及材料。

    6.
    发明专利
    未知

    公开(公告)号:DE523982T1

    公开(公告)日:1993-07-08

    申请号:DE92306490

    申请日:1992-07-15

    Abstract: A capillary electrophoresis element is disclosed. The elements includes a capillary electrophoresis tube containing a low-voscosity polymer solution having a selected mesh size and low-solution viscosity. The mesh size may range from 50-100 ANGSTROM , for separating single-stranded oligonucleotides, to up to 300 ANGSTROM or greater, for separating relatively large duplex DNA fragments or proteins. Also disclosed is a method for formulating a low-viscosoty electrophoresis separation medium having a selected mesh size.

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